A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21n100



Internal ID20151637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12775725..12954384hg38UCSC Ensembl
chr1:12835868..13015495hg19UCSC Ensembl
chr1:12758455..12938082hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38178660
hg19179628
hg18179628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011809, nsv1006654, nsv997632, nsv1010745, nsv998681, nsv1000920, nsv1006273, nsv1002288, nsv998530
Samples
Known GenesHNRNPCL1, LOC649330, PRAMEF1, PRAMEF10, PRAMEF11, PRAMEF12, PRAMEF2, PRAMEF4, PRAMEF6, PRAMEF7, PRAMEF8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv21n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss72
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer